» Articles » PMID: 23863401

Increased Body Mass Index is Associated with Earlier Time to Loss of Response to Infliximab in Patients with Inflammatory Bowel Disease

Overview
Specialty Gastroenterology
Date 2013 Jul 19
PMID 23863401
Citations 62
Authors
Affiliations
Soon will be listed here.
Abstract

Background: Obesity is an emerging problem in the care of inflammatory bowel disease (IBD) patients and has been associated with a diminished response to adalimumab. Whether obesity influences the response to infliximab (IFX) is not known.

Methods: A retrospective cohort of 124 subjects with IBD initiating IFX, naive to biologic therapy, was identified. Subjects were stratified according to their weight and body mass index (BMI). The primary outcome was the first occurrence of an IBD flare defined as dose escalation of IFX, corticosteroid use, discontinuation of IFX, hospitalization, or surgery. Multivariable logistic regression was performed considering body mass and BMI as categorical and continuous variables.

Results: Obese (BMI > 30 kg/m) patients with Crohn's disease were more likely to have an IBD flare than nonobese patients (adjusted hazard ratio [HR]: 3.03, P < 0.001); overweight (BMI > 25 kg/m) patients with ulcerative colitis trended toward a similar observation (HR: 9.68, P = 0.06). When considered as continuous variables, increasing mass and BMI were associated with earlier IBD flare in both Crohn's disease (adjusted HR: 1.06 per unit increase in BMI [P = 0.02] and 1.02 per kg increase in body mass [P = 0.02]) and ulcerative colitis (adjusted HR: 1.3 per unit increase in BMI [P = 0.01] and 1.11 per kg increase in body mass [P = 0.004]).

Conclusions: Increased body weight is associated with an earlier time to loss of response to IFX in Crohn's disease and ulcerative colitis, a novel finding given that IFX is the only antitumor necrosis factor agent whose dosing reflects increased body weight.

Citing Articles

Use of Glucagon-Like Peptide-1 Receptor Agonists in Patients With Inflammatory Bowel Disease.

Boumitri C Gastroenterol Hepatol (N Y). 2025; 21(1):59-61.

PMID: 39897342 PMC: 11784567.


Prevalence of Metabolic Syndrome and Its Association with Cardiovascular Outcomes in Hospitalized Patients with Inflammatory Bowel Disease.

Njeim R, Pannala S, Zaidan N, Habib T, Rajamanuri M, Moussa E J Clin Med. 2024; 13(22).

PMID: 39598052 PMC: 11594857. DOI: 10.3390/jcm13226908.


Paediatric obesity and Crohn's disease: a descriptive review of disease phenotype and clinical course.

McCoy J, Miller M, Watson M, Crowley E, Woolfson J Paediatr Child Health. 2024; 29(3):158-162.

PMID: 38827375 PMC: 11141610. DOI: 10.1093/pch/pxad065.


A High Visceral-to-Skeletal Muscle Area Ratio on Cross-Sectional Imaging Is Associated With Failure of Standard Ustekinumab Doses: A Multicenter Study.

Tan Z, Chin A, Welman C, Thin L Clin Transl Gastroenterol. 2024; 15(7):e00722.

PMID: 38822800 PMC: 11272374. DOI: 10.14309/ctg.0000000000000722.


Trajectory of body mass index and obesity in children with Crohn's disease compared to healthy children.

Mitchel E, Huang J, Zemel B, Baldassano R, Albenberg L, Denburg M J Pediatr Gastroenterol Nutr. 2024; 78(1):85-94.

PMID: 38291691 PMC: 11823676. DOI: 10.1002/jpn3.12063.